Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL

被引:68
作者
Reichel, M
Gillert, E
Angermüller, S
Hensel, JP
Heidel, F
Lode, M
Leis, T
Biondi, A
Haas, OA
Strehl, S
Panzer-Grümayer, ER
Griesinger, F
Beck, JD
Greil, J
Fey, GH
Uckun, FM
Marschalek, R
机构
[1] Univ Frankfurt, Bioctr, Inst Pharmaceut Biol, D-60439 Frankfurt, Germany
[2] Univ Erlangen Nurnberg, Chair Genet, D-91058 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Dept Pediat, D-91054 Erlangen, Germany
[4] Osped S Gerardo, Ctr Ric M Tettamanti, I-20052 Monza, MI, Italy
[5] St Anna Kinderspital, CCRI, A-1090 Vienna, Austria
[6] Univ Hosp Gottingen, Div Haematol Oncol, D-37075 Gottingen, Germany
[7] Parker Hughes Canc Ctr, St Paul, MN 55113 USA
[8] Parker Hughes Inst, Childrens Canc Grp, ALL Biol Reference Lab, St Paul, MN 55113 USA
关键词
chromosomal translocation t(4; 11); ALL-1/MLL/HRX gene; AF4; gene;
D O I
10.1038/sj.onc.1204401
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Derivative chromosomes of 40 patients diagnosed with t(4;11) acute lymphoblastic leukemia (ALL),were analysed on the genomic DNA level. Chromosomal breakpoints were identified in most cases within the known breakpoint cluster regions of the involved MLL and AF4 genes, Due to our current knowledge of the primary DNA sequences of both breakpoint cluster regions, specific features were identified at the chromosomal fusion sites, including deletions, inversions and duplications of parental DNA sequences, After separation of all t(4;11) leukemia patients into two age classes (below and above 1 year of age), the analysis of chromosomal fusion sites revealed significant differences in the distribution of chromosomal breakpoints and led to the definition of two hotspot areas within the MLL breakpoint cluster region, This may point to the possibility of different age-linked mechanisms that sere leading to t(4;11) chromosomal translocations. Oncogene (2001) 20, 2900-2907.
引用
收藏
页码:2900 / 2907
页数:8
相关论文
共 20 条
[1]   MOLECULAR-BASIS OF 11Q23 REARRANGEMENTS IN HEMATOPOIETIC MALIGNANT PROLIFERATIONS [J].
BERNARD, OA ;
BERGER, R .
GENES CHROMOSOMES & CANCER, 1995, 13 (02) :75-85
[2]  
Cimino G, 1997, CANCER RES, V57, P2879
[3]  
Cimino G, 1998, HAEMATOLOGICA, V83, P350
[4]   Panhandle polymerase chain reaction amplifies MLL genomic translocation breakpoint involving unknown partner gene [J].
Felix, CA ;
Kim, CS ;
Megonigal, MD ;
Slater, DJ ;
Jones, DH ;
Spinner, NB ;
Stump, T ;
Hosler, MR ;
Nowell, PC ;
Lange, BJ ;
Rappaport, EF .
BLOOD, 1997, 90 (12) :4679-4686
[5]   A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells [J].
Gillert, E ;
Leis, T ;
Repp, R ;
Reichel, M ;
Hösch, A ;
Breitenlohner, I ;
Angermüller, S ;
Borkhardt, A ;
Harbott, J ;
Lampert, F ;
Griesinger, F ;
Greil, J ;
Fey, GH ;
Marschalek, R .
ONCOGENE, 1999, 18 (33) :4663-4671
[6]  
GU Y, 1994, CANCER RES, V54, P2327
[7]   A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level [J].
Leis, T ;
Repp, R ;
Borkhardt, A ;
Metzler, M ;
Schläger, F ;
Harbott, J ;
Lampert, F .
LEUKEMIA, 1998, 12 (05) :758-763
[8]   The structure of the human ALL-1/MLL/HRX gene [J].
Marschalek, R ;
Nilson, I ;
Löchner, K ;
Greim, R ;
Siegler, G ;
Greil, J ;
Beck, JD ;
Fey, GH .
LEUKEMIA & LYMPHOMA, 1997, 27 (5-6) :417-+
[9]   MOLECULAR ANALYSIS OF THE CHROMOSOMAL BREAKPOINT AND FUSION TRANSCRIPTS IN THE ACUTE LYMPHOBLASTIC SEM CELL-LINE WITH CHROMOSOMAL TRANSLOCATION T(4-11) [J].
MARSCHALEK, R ;
GREIL, J ;
LOCHNER, K ;
NILSON, I ;
SIEGLER, G ;
ZWECKBRONNER, I ;
BECK, JD ;
FEY, GH .
BRITISH JOURNAL OF HAEMATOLOGY, 1995, 90 (02) :308-320
[10]   Exon/intron structure of the human ALL-1 (MLL) gene involved in translocations to chromosomal region 11q23 and acute leukaemias [J].
Nilson, I ;
Lochner, K ;
Siegler, G ;
Greil, J ;
Beck, JD ;
Fey, GH ;
Marschalek, R .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 (04) :966-972